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Stability-enhanced solid dispersion formulation of amorphous raloxifene hydrochloride

Authors
Cho, Chin SungShin, Taek HwanLim, Jong LaeMoon, Ki YoungKim, Duk KiChoi, Young Wook
Issue Date
Nov-2010
Publisher
KOREAN INSTITUTE CHEMICAL ENGINEERS
Keywords
Raloxifene; Polymorphs; Solid Dispersion; Stability; Dissolution
Citation
KOREAN JOURNAL OF CHEMICAL ENGINEERING, v.27, no.6, pp 1906 - 1909
Pages
4
Journal Title
KOREAN JOURNAL OF CHEMICAL ENGINEERING
Volume
27
Number
6
Start Page
1906
End Page
1909
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22127
DOI
10.1007/s11814-010-0409-y
ISSN
0256-1115
1975-7220
Abstract
To develop a stabilized formulation of amorphous raloxifene hydrochloride (RXF), solid dispersion granules (SDG) of amorphous RXF were prepared by fluidized bed granulation with non-pareil beads, compressed and film-coated to produce solid dispersion tablets (SDT). Polymorphic changes in RXF were inhibited by SDG formulation. Drug content, impurity, and dissolution profile of SDT revealed that the SDT meets the acceptance criteria, and the content of RXF was maintained over 95% for 5 months at accelerated conditions of 40 degrees C and 75% R.H. In comparative dissolution study of reference tablet (Evista (R)) and SDT, the similarity factor (f(2)) provided evidence for similar dissolution profiles between two formulations. Therefore, we suggest the usefulness of SDT for the development of generic pharmaceuticals containing amorphous RXF.
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